Canonical Allele Identifier: CA381554905

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258330G>A (hg19) ; chr11:g.67490859G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490859G>A , CM000673.2:g.67490859G>A	GRCh38
NC_000011.9:g.67258330G>A , CM000673.1:g.67258330G>A	GRCh37
NC_000011.8:g.67014906G>A	NCBI36
NG_008969.1:g.12826G>A , LRG_460:g.12826G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.1166G>A
ENST00000528641.7:c.670G>A	ENSP00000434982.3:p.Asp224Asn
ENST00000529797.2:n.1701G>A
ENST00000682324.1:c.469-138G>A	ENSP00000508017.1:n.469-138G>A
ENST00000682659.1:c.490G>A	ENSP00000507351.1:p.Asp164Asn
ENST00000682699.1:c.859G>A	ENSP00000507935.1:p.Asp287Asn
ENST00000683237.1:c.851G>A	ENSP00000507343.1:p.Ter284=
ENST00000683856.1:c.682G>A	ENSP00000507979.1:p.Asp228Asn
ENST00000684006.1:c.848G>A	ENSP00000507269.1:p.Ter283=
ENST00000684657.1:c.679G>A	ENSP00000507961.1:p.Asp227Asn
ENST00000279146.8:c.859G>A MANE Select	ENSP00000279146.3:p.Asp287Asn
ENST00000279146.7:c.859G>A	ENSP00000279146.3:p.Asp287Asn
ENST00000528641.6:c.670G>A	ENSP00000434982.2:p.Asp224Asn
NM_001302959.1:c.682G>A	NP_001289888.1:p.Asp228Asn
NM_001302960.1:c.851G>A	NP_001289889.1:p.Ter284=
NM_003977.3:c.859G>A	NP_003968.3:p.Asp287Asn
XM_024448761.1:c.859G>A	XP_024304529.1:p.Asp287Asn
NM_003977.4:c.859G>A MANE Select	NP_003968.3:p.Asp287Asn
NM_001302960.2:c.851G>A	NP_001289889.1:p.Ter284=
NM_001302959.2:c.682G>A	NP_001289888.1:p.Asp228Asn